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Evolutionary study of Yersinia genomes deciphers emergence of human pathogenic species

On record, there are 17 species in the Yersinia genus, of which three are known to be pathogenic to human. While the chromosomal and pYV (or pCD1) plasmid-borne virulence genes as well as pathogenesis of these three species are well studied, their genomic evolution is poorly understood. Our study ai...

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Autores principales: Tan, Shi Yang, Tan, Irene Kit Ping, Tan, Mui Fern, Dutta, Avirup, Choo, Siew Woh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5086877/
https://www.ncbi.nlm.nih.gov/pubmed/27796355
http://dx.doi.org/10.1038/srep36116
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author Tan, Shi Yang
Tan, Irene Kit Ping
Tan, Mui Fern
Dutta, Avirup
Choo, Siew Woh
author_facet Tan, Shi Yang
Tan, Irene Kit Ping
Tan, Mui Fern
Dutta, Avirup
Choo, Siew Woh
author_sort Tan, Shi Yang
collection PubMed
description On record, there are 17 species in the Yersinia genus, of which three are known to be pathogenic to human. While the chromosomal and pYV (or pCD1) plasmid-borne virulence genes as well as pathogenesis of these three species are well studied, their genomic evolution is poorly understood. Our study aims to predict the key evolutionary events that led to the emergence of pathogenic Yersinia species by analyzing gene gain-and-loss, virulence genes, and “Clustered regularly-interspaced short palindromic repeats”. Our results suggest that the most recent ancestor shared by the human pathogenic Yersinia was most probably an environmental species that had adapted to the human body. This might have led to ecological specialization that diverged Yersinia into ecotypes and distinct lineages based on differential gene gain-and-loss in different niches. Our data also suggest that Y. pseudotuberculosis group might be the donor of the ail virulence gene to Y. enterocolitica. Hence, we postulate that evolution of human pathogenic Yersinia might not be totally in parallel, but instead, there were lateral gene transfer events. Furthermore, the presence of virulence genes seems to be important for the positive selection of virulence plasmid. Our studies provide better insights into the evolutionary biology of these bacteria.
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spelling pubmed-50868772016-11-04 Evolutionary study of Yersinia genomes deciphers emergence of human pathogenic species Tan, Shi Yang Tan, Irene Kit Ping Tan, Mui Fern Dutta, Avirup Choo, Siew Woh Sci Rep Article On record, there are 17 species in the Yersinia genus, of which three are known to be pathogenic to human. While the chromosomal and pYV (or pCD1) plasmid-borne virulence genes as well as pathogenesis of these three species are well studied, their genomic evolution is poorly understood. Our study aims to predict the key evolutionary events that led to the emergence of pathogenic Yersinia species by analyzing gene gain-and-loss, virulence genes, and “Clustered regularly-interspaced short palindromic repeats”. Our results suggest that the most recent ancestor shared by the human pathogenic Yersinia was most probably an environmental species that had adapted to the human body. This might have led to ecological specialization that diverged Yersinia into ecotypes and distinct lineages based on differential gene gain-and-loss in different niches. Our data also suggest that Y. pseudotuberculosis group might be the donor of the ail virulence gene to Y. enterocolitica. Hence, we postulate that evolution of human pathogenic Yersinia might not be totally in parallel, but instead, there were lateral gene transfer events. Furthermore, the presence of virulence genes seems to be important for the positive selection of virulence plasmid. Our studies provide better insights into the evolutionary biology of these bacteria. Nature Publishing Group 2016-10-31 /pmc/articles/PMC5086877/ /pubmed/27796355 http://dx.doi.org/10.1038/srep36116 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Tan, Shi Yang
Tan, Irene Kit Ping
Tan, Mui Fern
Dutta, Avirup
Choo, Siew Woh
Evolutionary study of Yersinia genomes deciphers emergence of human pathogenic species
title Evolutionary study of Yersinia genomes deciphers emergence of human pathogenic species
title_full Evolutionary study of Yersinia genomes deciphers emergence of human pathogenic species
title_fullStr Evolutionary study of Yersinia genomes deciphers emergence of human pathogenic species
title_full_unstemmed Evolutionary study of Yersinia genomes deciphers emergence of human pathogenic species
title_short Evolutionary study of Yersinia genomes deciphers emergence of human pathogenic species
title_sort evolutionary study of yersinia genomes deciphers emergence of human pathogenic species
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5086877/
https://www.ncbi.nlm.nih.gov/pubmed/27796355
http://dx.doi.org/10.1038/srep36116
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